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Ciliary Neurotrophic Factor Induces Down-regulation of Its Receptor and Desensitization of Signal Transduction Pathways in Vivo
Despite the widespread use of polypeptide growth factors as pharmacological agents, little is known about the extent to which these molecules regulate their cognate cell surface receptors and signal transduction pathways in vivo . We have addressed this issue with respect to the neurotrophic molecul...
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Published in: | The Journal of biological chemistry 1996-09, Vol.271 (37), p.22839 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | Despite the widespread use of polypeptide growth factors as pharmacological agents, little is known about the extent to which
these molecules regulate their cognate cell surface receptors and signal transduction pathways in vivo . We have addressed this issue with respect to the neurotrophic molecule ciliary neurotrophic factor (CNTF). Administration
of CNTF in vivo resulted in modest decreases in levels of CNTFRα mRNA and protein in skeletal muscle. CNTF causes the rapid tyrosine phosphorylation
of LIFRβ and gp130 and the induction of the immediate-early gene, tis 11; injection of CNTF 3-7 h after an initial exposure failed to re-stimulate these immediate-early responses, suggesting a
biochemical desensitization to CNTF not accounted for by decreased receptor protein. To determine whether the desensitization
of immediate-early responses caused by CNTF resulted in a functional desensitization, we compared the efficacy of multiple daily injections versus a single daily dose of CNTF in preventing the denervation-induced atrophy of skeletal muscle. Surprisingly, injections of
CNTF every 6 h, which falls within the putative refractory period for biochemical responses, resulted in efficacy equal to
or greater than injections once daily. These results suggest that although much of the CNTF signal transduction machinery
is down-regulated with frequent CNTF dosing, biological signals continue to be recognized and interpreted by the cell. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.271.37.22839 |